- Integra LifeSciences (Plainsboro, NJ)
- …preferred + Experience: 6 to 8 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + Demonstrates ... outcomes and set new standards of care. The **Sr.** ** Quality Engineer - Medical Device ...and surveillance audits and customer audits. + Perform other Quality Assurance and Quality Engineering… more
- Integra LifeSciences (Plainsboro, NJ)
- …Electrical) + Experience: 3 to 6 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + Demonstrates ... and set new standards of care. **SUMMARY DESCRIPTION** The ** Quality Assurance Engineer II** will provide ...and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical… more
- Integra LifeSciences (Princeton, NJ)
- …Mechanical) or related discipline, with 5+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, or ... mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring… more
- Integra LifeSciences (Plainsboro, NJ)
- …Chemistry). + 2 to 6 years of experience in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. + Demonstrates ... candidate must be familiar with process flow of a medical device organization, including the regulatory impact...equipment. + Results oriented with a strong focus on quality principles and conflict resolution. + Excellent technical writing… more
- Merck (Rahway, NJ)
- …strategic partnerships with manufacturing sites and partner groups + Regulatory Compliance and Quality Assurance : + Ensure that all activities are conducted with ... Materials Engineering, or similar **Experience** **8+ years of experience in medical device or combination product engineering.** **Demonstrated technical… more
- Robert Half Technology (Mahwah, NJ)
- …and effectiveness of documentation systems. * Support compliance with medical device regulations and quality assurance standards. * Collaborate with ... Description We are looking for a dedicated Regulatory Affairs Quality Assurance Specialist to join our team...management systems. * Solid understanding of quality assurance principles and regulatory requirements for medical … more
- Organon & Co. (Jersey City, NJ)
- …of global GMP Quality Systems and regulatory requirements. + Experience in medical device Quality Systems is preferred, including familiarity with ... responsible for ensuring that all Organon products managed by External Quality Assurance (EQA) are manufactured, packaged, analyzed, released, stored,… more
- Integra LifeSciences (Princeton, NJ)
- … mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring ... accuracy and sustainability of supplier requirements as they pertain to sterility assurance and drive cross-functional collaboration with supplier quality groups… more
- Integra LifeSciences (Plainsboro, NJ)
- …The ** Quality Inspector I** will be responsible for performing quality assurance inspections on purchased components, manufactured sub-assemblies and final ... product. The Quality Inspector will perform all duties in accordance to...corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable… more
- Integra LifeSciences (Plainsboro, NJ)
- …The ** Quality Inspector I** will be responsible for performing quality assurance inspections on purchased components, manufactured sub-assemblies and final ... product. The Quality Inspector will perform all duties in accordance to...corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable… more